ライフサイエンスコーパス: transmembrane receptor

1 oupled receptors (GPCRs, also known as seven-transmembrane receptors).

2 the neuropeptide sensitivity of the neuronal transmembrane receptor.

3 ai signaling module by a cell surface, seven-transmembrane receptor.

4 NA injection by T5 phage upon binding to its transmembrane receptor.

5 i) signaling module by a cell surface, seven-transmembrane receptor.

6 y similar defects as the knockout of the Dcc transmembrane receptor.

7 function are G proteins controlled by seven transmembrane receptors.

8 receptors (GPCRs) are the largest family of transmembrane receptors.

9 (Galpha), most notably by G protein-coupled transmembrane receptors.

10 g pathways initiated by specific nuclear and transmembrane receptors.

11 stributed in the cytoplasmic domains of many transmembrane receptors.

12 tein that connects the actin cytoskeleton to transmembrane receptors.

13 connections by anchoring actin filaments to transmembrane receptors.

14 ptor tyrosine kinase, and the Frizzled seven-transmembrane receptors.

15 c lipids may modulate ectodomain shedding of transmembrane receptors.

16 nly at the carboxyl tails of GPCRs and other transmembrane receptors.

17 with the same charge density but no specific transmembrane receptors.

18 tch family consists of four highly conserved transmembrane receptors.

19 lowing their recruitment to signal-activated transmembrane receptors.

20 degradation, a pathway usually reserved for transmembrane receptors.

21 mains in extracytoplasmic regions in several transmembrane receptors.

22 In addition to the 7 transmembrane receptor (7TM)-conserved disulfide bridge

23 Members of the seven-transmembrane receptor (7TMR) superfamily are sequestere

24 Ubiquitously expressed seven-transmembrane receptors (7TMRs) classically signal throu

25 Seven transmembrane receptors (7TMRs) exert strong regulatory

26 Seven-transmembrane receptors (7TMRs) have evolved in prokaryo

27 estin-mediated signaling downstream of seven transmembrane receptors (7TMRs) is a relatively new para

28 Seven transmembrane receptors (7TMRs), also known as G-protein

29 Seven-transmembrane receptors (7TMRs), also termed G protein-c

30 upled receptors (GPCRs), also known as seven-transmembrane receptors (7TMRs), both by inhibiting clas

31 Seven transmembrane receptors (7TMRs), commonly referred to as

32 ation, and some signaling functions of seven-transmembrane receptors (7TMRs).

33 e important roles in the regulation of seven-transmembrane receptors (7TMRs).

34 ated G protein-coupled receptors, (aka seven-transmembrane receptors, 7TMRs) also mediate 7TMR intern

35 Ligands acting at 7-transmembrane receptors (7TMs) transduce effects on cell

36 e first to reveal, we believe, for any seven-transmembrane receptor, a functional role of ubiquitinat

37 s, and our findings suggest that single pass transmembrane receptors act as GPCRs in plants, challeng

38 , for spatiotemporal control over endogenous transmembrane receptor activation, enabled through the o

39 talin are key steps to initiate the integrin transmembrane receptors' activation, which mediates many

40 med "energy taxis." In Escherichia coli, the transmembrane receptor Aer is the primary energy sensor

41 inducing peptide (AIP) signal to its cognate transmembrane receptor (AgrC) is responsible for control

42 oinducing peptides (AIPs)) and their cognate transmembrane receptors (AgrCs).

43 Expression of the cellular transmembrane receptor alphavbeta6 integrin is essential

44 that netrin-1 also interacts with the orphan transmembrane receptor amyloid precursor protein (APP).

45 ing cellular cytoprotective functions by a 7-transmembrane receptor and define the biochemical pathwa

46 bilical cord vascular endothelial cells as a transmembrane receptor and may recognize certain bacteri

47 Tissue factor (TF) is a transmembrane receptor and primary initiator of blood co

48 otein expression and activation of NOTCH2, a transmembrane receptor and transcriptional regulator kno

49 structural and signaling scaffold that binds transmembrane receptors and a wide variety of intracellu

50 nctions through binding to ligand-stimulated transmembrane receptors and activating their kinase doma

51 located within the cytoplasmic tails of many transmembrane receptors and associated adaptor proteins

52 nally important bridging interaction between transmembrane receptors and histidine kinase.

53 Merlin associates with several transmembrane receptors and intracellular proteins servi

54 bly and intracellular trafficking of various transmembrane receptors and ion-transport proteins.

55 d shedding extracellular domains of multiple transmembrane receptors and ligands.

56 IGF actions are mediated by transmembrane receptors and modulated by IGF-binding pro

57 d receptors (GPCRs) are the largest class of transmembrane receptors and serve as signal mediators to

58 Rs) represent one of the largest families of transmembrane receptors and the most common drug target.

59 manner that required selective activation of transmembrane receptors and was distinct from VEGF-A-ind

60 ure accurate trafficking and distribution of transmembrane receptors and/or proteins and their ligand

61 Heart of Glass (HEG1), a transmembrane receptor, and Rasip1, an endothelial-speci

62 e last 20 years support the notion that some transmembrane receptors are activated not only by their

63 In many sensory systems, transmembrane receptors are spatially organized in large

64 Transmembrane receptors are the predominant conduit thro

65 oupled receptors (GPCRs, also known as seven-transmembrane receptors) are typically found at the cell

66 TLRs), widely expressed and highly conserved transmembrane receptors, are at the intersection of diet

67 In this model, Smo acts like many transmembrane receptors associated with cytoplasmic kina

68 response, which involves activation of three transmembrane receptors, ATF6, PERK and IRE1alpha.

69 PAR1 is a biased 7-transmembrane receptor because G proteins mediate thromb

70 ance of C5a receptor [(C5aR)2/C5L2], a seven-transmembrane receptor binding C5a and C5adesArg, remain

71 fat encodes a transmembrane receptor, but post-translational regulatio

72 etween extracellular signaling molecules and transmembrane receptors, but how appropriate context-dep

73 Cleavage of transmembrane receptors by gamma-secretase is the final

74 esicles maintain the structural integrity of transmembrane receptors by keeping them in their physiol

75 ation of heterodimeric (alpha/beta) integrin transmembrane receptors by the 270 kDa cytoskeletal prot

76 echanism by which an anti-inflammatory seven-transmembrane receptor can negatively regulate JAK/STAT

77 e recent discoveries reveal the existence of transmembrane receptors capable of responding to steroid

78 rotein is necessary for transit of selective transmembrane receptor cargo by the COPII coat for anter

79 CCL21 are endogenous agonists for the seven-transmembrane receptor CCR7.

80 d for several genes, including those for the transmembrane receptor CD44 (CD44 [rs507230]; P = 3.98 x

81 ar carbohydrate-binding domain of the Type I transmembrane receptor CD44 is known to undergo affinity

82 nce suggests that interactions involving the transmembrane receptor CD44 may play an important role i

83 MIF (which largely functions via the type II transmembrane receptor CD74) in prostate, bladder and ki

84 CRT together with the transmembrane receptor CD91 function at the cell membran

85 We identify the transmembrane receptor Celsr3/Adgrc3 as a binding partne

86 netic disorder, is caused by mutations of CF transmembrane receptor (CFTR) - a chloride channel prese

87 way as a result of defective cystic fibrosis transmembrane receptor (CFTR) expression and function.

88 d for inferring the functional properties of transmembrane receptor clusters from their structure.

89 ndothelial growth factor receptor, Flt1 is a transmembrane receptor co-expressed with an alternate tr

90 Integrins are transmembrane receptors composed of alpha and beta subun

91 Integrins are transmembrane receptors composed of one alpha subunit an

92 Integrins are heterodimeric transmembrane receptors consisting of alpha and beta sub

93 e multiple physiologic systems by activating transmembrane receptors containing intracellular guanyly

94 and detect their concentration via the AgrC transmembrane receptor, coordinating local bacterial pop

95 Here, we show that a transmembrane receptor, DCC, forms a binding complex con

96 Here we show that netrin-1 via its transmembrane receptors, deleted in colorectal cancer an

97 Notch transmembrane receptors direct essential cellular proces

98 and through the neuronal leucine-rich repeat transmembrane receptor DMA-1 on sensory dendrites.

99 kin, SAX-7/L1CAM and MNR-1, and the neuronal transmembrane receptor DMA-1.

100 norhabditis elegans through the leucine-rich transmembrane receptor DMA-1/LRR-TM expressed on PVD neu

101 peptide ligand that binds and activates the transmembrane receptor domain, eliciting a cellular casc

102 ators interact with aromatic residues in the transmembrane receptor domain.

103 ues, we developed a phenotyping asssay named Transmembrane Receptor Dynamics (TReD), studied the dyna

104 ines and developed a phenotyping assay named Transmembrane Receptor Dynamics (TReD).

105 hat are involved in the glycosylation of the transmembrane receptor dystroglycan.

106 including the upregulated expression of the transmembrane receptor endosialin (CD248).

107 The gene identified encodes a putative transmembrane receptor expressed in all tissues capable

108 iate many of their physiological effects via transmembrane receptors expressed in the plasma membrane

109 eptors (MORs) are members of the large seven-transmembrane receptor family which transduce the effect

110 llular loops in structural studies of this 7 transmembrane receptor family.

111 We showed that the seven-transmembrane receptor fAR1 is required for folic acid-m

112 ved signaling node comprising a prototypical transmembrane receptor for c-di-GMP, LapD, and a cognate

113 Here we report that the CD44, a transmembrane receptor for hyaluronan, modulates synapti

114 Megalin is a transmembrane receptor for serum d-binding protein (DBP)

115 Mice lacking the CD44 transmembrane receptor for the glycosaminoglycan hyaluro

116 or-like tyrosine kinase (RYK) functions as a transmembrane receptor for the Wnt family of secreted pr

117 The activin receptor type IIB (ActRIIB) is a transmembrane receptor for transforming growth factor-be

118 ughput technology to interrogate most single transmembrane receptors for binding to 445 IgSF proteins

119 radation of bri1-9 and bri1-5, two defective transmembrane receptors for brassinosteroids.

120 The integrins are transmembrane receptors for ECM proteins, and they regul

121 Mammalian plexins constitute a family of transmembrane receptors for semaphorins and represent cr

122 The internalization of transmembrane receptors from the cell surface plays a ce

123 of a physiological requirement for ER-QC in transmembrane receptor function in plants.

124 milarities and their ability to activate the transmembrane receptor glycoprotein 130 (gp130).

125 In this study, we show that a seven-transmembrane receptor, GPR17, negatively regulates the

126 results provide atomic insight into a type I transmembrane receptor heterocomplex and the mechanism o

127 ggest entry into neuronal stem cells through transmembrane receptors, hijacking cellular signaling to

128 s to reveal the arrangement of the component transmembrane receptors, histidine kinases (CheA) and Ch

129 The repeating ternary units are composed of transmembrane receptors, histidine-kinase CheA, and coup

130 Classic IL-6 signaling is conditioned by the transmembrane receptor (IL-6R) and homodimerization of g

131 ycation end products (RAGE) is a multiligand transmembrane receptor implicated in a number of disease

132 e of an intrinsically disordered region of a transmembrane receptor in long-range allostery.

133 We screened all LRR-containing transmembrane receptors in C. elegans and identified the

134 ch encodes an emerging positive regulator of transmembrane receptors in plants, suppressed the effect

135 show that somatodendritic sorting of various transmembrane receptors in rat hippocampal neurons is me

136 eriments, we investigated the roles of three transmembrane receptors in regulating dorsolateral pathf

137 Members of the plexin family are unique transmembrane receptors in that they interact directly w

138 We investigated the role of CD44, a transmembrane receptor, in mediating MSU phagocytosis by

139 t spatio-temporal localization of Kremen1, a transmembrane receptor, in the mammalian cochlea, and in

140 le photocontrol of the clustering of diverse transmembrane receptors including fibroblast growth fact

141 onse to the triggering of a diverse array of transmembrane receptors, including antigen receptors.

142 l lamina is linked to the sarcolemma through transmembrane receptors, including integrins and dystrog

143 lasma membrane to cytoskeleton by binding to transmembrane receptor integrin and actin.

144 Activation of transmembrane receptor integrin by talin is essential fo

145 ase (ILK) plays a pivotal role in connecting transmembrane receptor integrin to the actin cytoskeleto

146 Transmembrane receptors interact with extracellular liga

147 arge class of soluble proteins that dimerize transmembrane receptors into precise signaling topologie

148 Notch1 is an evolutionarily conserved transmembrane receptor involved in melanoma growth.

149 which signals through cAMP, is a melanocytic transmembrane receptor involved in pigmentation, adaptiv

150 ceptor CXC-chemokine receptor 4 (CXCR4) is a transmembrane receptor involved in survival, proliferati

151 Fas is a transmembrane receptor involved in the maintenance of to

152 c embryogenesis receptor kinases (SERKs) are transmembrane receptors involved in plant immunity.

153 Notch are transmembrane receptors involved in the determination of

154 ession requires the RNase activity of the ER transmembrane receptor IRE-1, we developed a potent IRE-

155 The endoplasmic reticulum transmembrane receptor Ire1 senses over-accumulation of

156 Proteolysis of transmembrane receptors is a critical cellular communica

157 In nonneuronal cells, CME of the majority of transmembrane receptors is either directly or indirectly

158 FR trafficking, as the localization of other transmembrane receptors is unaltered in chp-1(lf) mutant

159 Robo1, a single-pass transmembrane receptor, is crucial for neuronal guidance

160 rol-dependent nanoclustering of cell surface transmembrane receptor kinase 1 (TMK1) is critical for t

161 Flagellin sensing2 (FLS2) is a transmembrane receptor kinase that activates antimicrobi

162 n AvrPto does so by directly targeting plant transmembrane receptor kinases involved in bacterial per

163 Smads, through C-terminal phosphorylation by transmembrane receptor kinases.

164 sduction pathway involving the BRI1 and BAK1 transmembrane receptor kinases.

165 plasmic levels of cyclic-di-GMP activate the transmembrane receptor LapD that in turn recruits the pe

166 Transmembrane receptor-like kinases characterized by the

167 BG1 encodes an Ig-superfamily type I transmembrane receptor-like protein that contains an imm

168 There are many transmembrane receptor-like proteins whose ligands have

169 These transmembrane receptors, localized at the cellular or en

170 ntify GRK5/6 as novel kinases for the single transmembrane receptor LRP6 during Wnt signaling.

171 MKS3, encoding the transmembrane receptor meckelin, is mutated in Meckel-Gr

172 Mutations in the gene encoding the single transmembrane receptor multiple epidermal growth factor-

173 to heightened inflammatory responses from CF transmembrane receptor mutant cells and highlight autoph

174 or complex of distinct Lys motif (LysM)-type transmembrane receptors named NOD FACTOR RECEPTOR1 (LjNF

175 Release of HJV requires it to bind to the transmembrane receptor neogenin.

176 Mice that lack the transmembrane receptor neuropilin-1 (Nrp1), which modula

177 The role of the transmembrane receptor Notch in the adult brain is poorl

178 Signaling through the transmembrane receptor Notch is widely used throughout a

179 microvessels to show that activation of the transmembrane receptor NOTCH1 directly regulates vascula

180 Members of the Notch family of transmembrane receptors, Notch1-4 in mammals, are involv

181 Deleted in colorectal cancer (DCC), a large transmembrane receptor of netrin-1, is critical for medi

182 ike domain containing receptor 1, a putative transmembrane receptor of unknown function.

183 Interaction of transmembrane receptors of the Robo family and the secre

184 The vibrio autoinducer molecules bind to transmembrane receptors of the two-component histidine s

185 Cell surface transmembrane receptors often form nanometer- to microme

186 Atypical 7-transmembrane receptors, often called decoy receptors, a

187 where raft compartmentalization can promote transmembrane receptor oligomerization, shield proteins

188 specific GAG sulfation patterns and involve transmembrane receptors or extracellular matrix-associat

189 otile bacteria sense chemical gradients with transmembrane receptors organised in supramolecular sign

190 ions by binding to a G protein-coupled seven-transmembrane receptor (PAFR).

191 (mRNA) expression of Indian Hh, a ligand of transmembrane receptor patched 1, was 184x higher in BE

192 d in a non-redundant fashion with the Draper transmembrane receptor pathway: loss of either pathway f

193 Cell transmembrane receptors play a key role in the detection

194 ted semaphorin 2b (Sema-2b) acts through its transmembrane receptor Plexin B (PlexB) to locally attra

195 , renal tubular epithelial cells lacking the transmembrane receptor Plexin-B2 or its semaphorin ligan

196 orin 3E (Sema3E), acts through a single-pass transmembrane receptor, plexin D1, to provide a repulsiv

197 s undergoes structural rearrangements as the transmembrane receptor protein is activated.

198 The transmembrane receptor protein neuropilin 1 (Nrp1) was r

199 learning rate, of the collagen formation and transmembrane receptor protein tyrosine kinase activity

200 positional cloning and report it to encode a transmembrane receptor protein with two hypervariable ex

201 Transmembrane receptors recognize conserved pathogen-ass

202 erial chemotaxis signaling cluster, in which transmembrane receptors regulate CheA autokinase activit

203 homodimerization and heterodimerization of 7-transmembrane receptors regulate processes including spe

204 However, identifying transmembrane receptors remains challenging.

205 RIIa) has been identified as an ITAM-bearing transmembrane receptor responsible for mediating "outsid

206 These arrays can be formed around transmembrane receptors, resulting in arrays embedded in

207 Applying our approach to integrin transmembrane receptors revealed a spatial density gradi

208 The secreted protein, Slit2, and its transmembrane receptor, Robo-1, repel neuronal migration

209 ted neurorepellent Slit2, acting through its transmembrane receptor, Roundabout (Robo)-1, inhibits ch

210 discovery over 20 years ago, eukaryotic-like transmembrane receptor Ser/Thr protein kinases (STPKs) h

211 ondins (TSP or THBS) and the Notch family of transmembrane receptors share a role in multiple, overla

212 Members of the Frizzled family of sevenpass transmembrane receptors signal via the canonical Wnt pat

213 ce of membrane nanodomains in the control of transmembrane receptor signaling in vivo.

214 ents of signal transduction, cell cycle, and transmembrane receptor signaling pathways.

215 overed for their role in desensitizing seven-transmembrane receptor signaling via the heterotrimeric

216 how membrane nanoscale organization controls transmembrane receptors signaling activity remains a cha

217 ted that these glycoproteins would influence transmembrane receptor spatial organization and function

218 However, signaling via the transmembrane receptor ST2 and documented caspase-depend

219 been clarified despite recent advances in 7 transmembrane receptor structural biology.

220 Signaling by transmembrane receptors such as G protein-coupled recept

221 pattern recognition receptors-which include transmembrane receptors such as toll-like receptors (TLR

222 " Their receptors are part of a larger seven-transmembrane receptor superfamily, commonly referred to

223 nt component, C5a, binds two different seven-transmembrane receptors termed C5aR1 and C5aR2.

224 nd colleagues have identified a novel 17-kDa transmembrane receptor, termed Plg-R(KT), that binds pla

225 are signalling molecules, which activate the transmembrane receptor TGR5 and the nuclear receptor FXR

226 Podoplanin (PDPN) is a transmembrane receptor that affects the activities of Rh

227 ycation end products (RAGE) is a multiligand transmembrane receptor that can undergo proteolysis at t

228 The Nogo-B receptor (NgBR) is a transmembrane receptor that contains a conserved hydroph

229 Notch is a transmembrane receptor that controls a diverse array of

230 GPER is a G(s)-coupled seven-transmembrane receptor that has been linked to specific

231 RET encodes a transmembrane receptor that is 20 exons long and produce

232 The Notch gene encodes a transmembrane receptor that is cleaved upon activation,

233 (Spz) into the activating ligand for Toll, a transmembrane receptor that is distributed throughout th

234 GPR119 is a 7-transmembrane receptor that is expressed in the enteroen

235 ate Cyclase C (GC-C) is an apically-oriented transmembrane receptor that is expressed on epithelial c

236 Guanylate cyclase C (GC-C) is a transmembrane receptor that is expressed primarily on in

237 umor necrosis factor receptor 2 (TNFR2) is a transmembrane receptor that is linked to immune modulati

238 ial cells, guanylyl cyclase 2C (GUCY2C) is a transmembrane receptor that makes cGMP in response to th

239 Cadherin is a cell-surface transmembrane receptor that mediates calcium-dependent c

240 AIL-R1; also known as death receptor 4) is a transmembrane receptor that mediates TRAIL-induced apopt

241 PlexinD1, a transmembrane receptor that regulates neuronal and cardi

242 Robo4 is an endothelial-specific transmembrane receptor that stabilizes the vasculature,

243 eceptor 5 (DR5) is a death domain-containing transmembrane receptor that triggers apoptosis upon bind

244 eptor (LIMR)-type proteins are putative nine-transmembrane receptors that are evolutionarily conserve

245 Integrins are heterodimeric, transmembrane receptors that are expressed in all cells,

246 Unlike many transmembrane receptors that belong to large, extensivel

247 Neuropilins (NRPs) are transmembrane receptors that bind class 3 semaphorins an

248 Plexins are single-pass transmembrane receptors that bind the axon guidance mole

249 CD44 comprises a family of transmembrane receptors that can give rise to multiple C

250 Notch proteins are a family of transmembrane receptors that coordinate binary cell fate

251 Integrins are transmembrane receptors that have a pivotal role in mech

252 egrins comprise a family of 24 heterodimeric transmembrane receptors that mediate cell attachment to

253 Notch family members are transmembrane receptors that mediate essential developme

254 TPsigma) and its subfamily member LAR act as transmembrane receptors that mediate growth inhibition o

255 Cadherins are transmembrane receptors that mediate intercellular adhes

256 Integrins are bidirectional, allosteric transmembrane receptors that play a central role in hemo

257 TLRs are pattern recognition transmembrane receptors that play key roles in innate im

258 Notch receptors are transmembrane receptors that regulate cell fate decision

259 Plexins are transmembrane receptors that regulate processes such as

260 dulators is controlled by endocytosis of the transmembrane receptors that transduce their effects.

261 are made possible by integrins, a family of transmembrane receptors that, upon binding to the extrac

262 otective signaling stimulated by a typical 7-transmembrane receptor the angiotensin ATII 1A receptor,

263 l lattice formed from three core proteins: a transmembrane receptor, the His kinase CheA, and the ada

264 in is one of the most mechanistically direct transmembrane receptors-the intracellular domain contain

265 aling proteins, cytoskeletal components, and transmembrane receptors, thereby serving as a scaffold t

266 The primary initiator of coagulation, the transmembrane receptor tissue factor (TF), has gained co

267 ression of the proangiogenic/protumourigenic transmembrane receptor Tissue Factor.

268 nteractions that promoted the endocytosis of transmembrane receptors, TLR4 was selected as cargo for

269 After internalization, transmembrane receptors (TMRs) are typically recycled ba

270 Trafficking of transmembrane receptors to a specific intracellular comp

271 s relay extracellular cues from heptahelical transmembrane receptors to downstream effector molecules

272 s of studies, namely the propensity of seven transmembrane receptors to form dimers and thus demonstr

273 cellular matrix proteins, secreted cues, and transmembrane receptors to regulate axon guidance.

274 extracellular microenvironment by anchoring transmembrane receptors to the actin filaments.

275 Filamin-mediated linkages between transmembrane receptors (TR) and the actin cytoskeleton

276 rom the cytosol, including cell division and transmembrane receptor trafficking and degradation.

277 Derailed transmembrane receptor trafficking could be a hallmark o

278 The Notch family of transmembrane receptors transduce extracellular signals

279 vity upon binding to either or both distinct transmembrane receptors TrkA and p75(NTR).

280 BDNF signaling via its transmembrane receptor TrkB has an important role in neu

281 ms was observed for NTRK2, which encodes the transmembrane receptor tropomyosin-related kinase B, bin

282 TrkA is a cell surface transmembrane receptor tyrosine kinase for nerve growth

283 mutations and amplification of the type III transmembrane receptor tyrosine kinase KIT.

284 VEGFR-3 is a transmembrane receptor tyrosine kinase that is activated

285 ErbB4, a type I transmembrane receptor tyrosine kinase, is a member of t

286 or receptor (EGFR) is a heavily glycosylated transmembrane receptor tyrosine kinase.

287 unction through the insulin receptor (IR), a transmembrane receptor tyrosine kinase.

288 Here we show that the transmembrane receptor tyrosine phosphatase Leukocyte-an

289 Epidermal growth factor receptor (EGFR) is a transmembrane receptor-tyrosine kinase that is associate

290 Dimerization of single span transmembrane receptors underlies their mechanism of act

291 -unstimulated cells overexpressing the seven transmembrane receptor vasopressin 2.

292 RDC3 and ARRDC4 upon activation of the seven transmembrane receptors vasopressin 2 and beta adrenergi

293 pression of Notch3, a member of Notch family transmembrane receptors, was elevated in human cells dur

294 Seven transmembrane receptors were originally named and charac

295 FZD5 encodes a transmembrane receptor with a conserved extracellular cy

296 Neuropilin-1 (NRP1) is an essential transmembrane receptor with a variety of cellular functi

297 gene encodes an approximately 50 kDa type I transmembrane receptor with an ectodomain containing thr

298 Plexin C1 is a type I transmembrane receptor with intrinsic R-Ras GTPase activ

299 human cytomegalovirus (HCMV)-encoded type I transmembrane receptors with Fcgamma-binding properties

300 herefore hypothesized that preorganizing the transmembrane receptors would potentiate local TGF-beta